ABOUT #MEACTION UK

Our movement fights for recognition, education, and research so that one day all people with ME (myalgic encephalomyelitis) will have access to rapid diagnosis, and compassionate, effective care. As people with ME, carers and allies ourselves, we campaign on the issues that are most pressing. 

In Scotland, health is a devolved issue for the Scottish Parliament and covered by #MEAction Scotland.

Our Work

TAKE ACTION NOW

Actions

TWO WEEKS TO SEND IN YOUR RESEARCH IDEAS

Help prioritise ME/CFS research by filling in this survey A major UK project is looking for your input. They want to know what research you think should be funded in the future, and the deadline for adding your ideas is fast approaching. Your responses must be in by Monday 5th July 2021. Find out more

Read More »

Get Involved in Campaigning

We are always looking for volunteers with ME and healthy allies to join our team. If you are interested in helping or getting involved click on the photo to contact us today.

MEET YOUR MP

Check out our guide to meeting your Member of Parliament (MP). Click the photo to find tips, suggestions, asks and sample language to meet your MP. It will give you the basic tools to help you to feel comfortable meeting with your MP.

Your experiences of ME Services - #MEAction UK

Explore OUR RESOURCES

Take a look through the resources our volunteers have created to help you understand our work, as well as factsheets and guides to enable you to take action.

Latest News

TWO WEEKS TO SEND IN YOUR RESEARCH IDEAS

Help prioritise ME/CFS research by filling in this survey A major UK project is looking for your input. They want to know what research you think should be funded in the future, and the deadline for adding your ideas is fast approaching. Your responses must be in by Monday 5th July 2021. Find out more

Read More »

Global media tells the story of the #Millionsmissing

We are thrilled to see the press tell our story of the #MillionsMissing this year, and the #MillionsMore “long haulers” expected to develop ME/CFS following a COVID-19 infection.   In Pittsburgh, a mother of four told her story in the Tribune-Review about her 25-year journey of never recovering after contracting EBV, the virus that causes Mono.

Read More »

Explore our UK resources

CONTACT THE UK TEAM

Looking to contact someone else? Contact the global team here, or the Scotland team here.

Support our work!

Donate now to support #MEAction UK.

Scroll to Top